US5011695A - Sterilization of blood and its derivatives with vitamins - Google Patents
Sterilization of blood and its derivatives with vitamins Download PDFInfo
- Publication number
- US5011695A US5011695A US07/311,483 US31148389A US5011695A US 5011695 A US5011695 A US 5011695A US 31148389 A US31148389 A US 31148389A US 5011695 A US5011695 A US 5011695A
- Authority
- US
- United States
- Prior art keywords
- vitamin
- treatment
- sterilizing agent
- plasma
- virus
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
- 229940088594 vitamin Drugs 0.000 title claims abstract description 20
- 229930003231 vitamin Natural products 0.000 title claims abstract description 20
- 235000013343 vitamin Nutrition 0.000 title claims abstract description 20
- 239000011782 vitamin Substances 0.000 title claims abstract description 20
- 230000001954 sterilising effect Effects 0.000 title claims abstract description 12
- 210000004369 blood Anatomy 0.000 title claims abstract description 10
- 239000008280 blood Substances 0.000 title claims abstract description 10
- 238000004659 sterilization and disinfection Methods 0.000 title description 10
- 238000000034 method Methods 0.000 claims abstract description 33
- GVJHHUAWPYXKBD-UHFFFAOYSA-N (±)-α-Tocopherol Chemical compound OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-UHFFFAOYSA-N 0.000 claims description 12
- 150000003722 vitamin derivatives Chemical class 0.000 claims description 12
- 235000010482 polyoxyethylene sorbitan monooleate Nutrition 0.000 claims description 11
- 229920000053 polysorbate 80 Polymers 0.000 claims description 11
- 239000003206 sterilizing agent Substances 0.000 claims description 11
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 claims description 9
- 239000000126 substance Substances 0.000 claims description 8
- ZAKOWWREFLAJOT-CEFNRUSXSA-N D-alpha-tocopherylacetate Chemical compound CC(=O)OC1=C(C)C(C)=C2O[C@@](CCC[C@H](C)CCC[C@H](C)CCCC(C)C)(C)CCC2=C1C ZAKOWWREFLAJOT-CEFNRUSXSA-N 0.000 claims description 7
- ZAKOWWREFLAJOT-UHFFFAOYSA-N d-alpha-Tocopheryl acetate Natural products CC(=O)OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1C ZAKOWWREFLAJOT-UHFFFAOYSA-N 0.000 claims description 7
- 229940042585 tocopherol acetate Drugs 0.000 claims description 7
- 239000011715 vitamin B12 Substances 0.000 claims description 7
- 229930003427 Vitamin E Natural products 0.000 claims description 6
- AGVAZMGAQJOSFJ-WZHZPDAFSA-M cobalt(2+);[(2r,3s,4r,5s)-5-(5,6-dimethylbenzimidazol-1-yl)-4-hydroxy-2-(hydroxymethyl)oxolan-3-yl] [(2r)-1-[3-[(1r,2r,3r,4z,7s,9z,12s,13s,14z,17s,18s,19r)-2,13,18-tris(2-amino-2-oxoethyl)-7,12,17-tris(3-amino-3-oxopropyl)-3,5,8,8,13,15,18,19-octamethyl-2 Chemical compound [Co+2].N#[C-].[N-]([C@@H]1[C@H](CC(N)=O)[C@@]2(C)CCC(=O)NC[C@@H](C)OP(O)(=O)O[C@H]3[C@H]([C@H](O[C@@H]3CO)N3C4=CC(C)=C(C)C=C4N=C3)O)\C2=C(C)/C([C@H](C\2(C)C)CCC(N)=O)=N/C/2=C\C([C@H]([C@@]/2(CC(N)=O)C)CCC(N)=O)=N\C\2=C(C)/C2=N[C@]1(C)[C@@](C)(CC(N)=O)[C@@H]2CCC(N)=O AGVAZMGAQJOSFJ-WZHZPDAFSA-M 0.000 claims description 6
- 239000012141 concentrate Substances 0.000 claims description 6
- WIGCFUFOHFEKBI-UHFFFAOYSA-N gamma-tocopherol Natural products CC(C)CCCC(C)CCCC(C)CCCC1CCC2C(C)C(O)C(C)C(C)C2O1 WIGCFUFOHFEKBI-UHFFFAOYSA-N 0.000 claims description 6
- 239000011726 vitamin B6 Substances 0.000 claims description 6
- 229940046009 vitamin E Drugs 0.000 claims description 6
- 235000019165 vitamin E Nutrition 0.000 claims description 6
- 239000011709 vitamin E Substances 0.000 claims description 6
- FPIPGXGPPPQFEQ-BOOMUCAASA-N Vitamin A Natural products OC/C=C(/C)\C=C\C=C(\C)/C=C/C1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-BOOMUCAASA-N 0.000 claims description 5
- 239000000203 mixture Substances 0.000 claims description 5
- ZUFQODAHGAHPFQ-UHFFFAOYSA-N pyridoxine hydrochloride Chemical compound Cl.CC1=NC=C(CO)C(CO)=C1O ZUFQODAHGAHPFQ-UHFFFAOYSA-N 0.000 claims description 5
- 229960000342 retinol acetate Drugs 0.000 claims description 5
- 235000019173 retinyl acetate Nutrition 0.000 claims description 5
- QGNJRVVDBSJHIZ-QHLGVNSISA-N retinyl acetate Chemical compound CC(=O)OC\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C QGNJRVVDBSJHIZ-QHLGVNSISA-N 0.000 claims description 5
- 239000011770 retinyl acetate Substances 0.000 claims description 5
- 235000019155 vitamin A Nutrition 0.000 claims description 5
- 239000011719 vitamin A Substances 0.000 claims description 5
- 239000011718 vitamin C Substances 0.000 claims description 5
- FPIPGXGPPPQFEQ-UHFFFAOYSA-N 13-cis retinol Natural products OCC=C(C)C=CC=C(C)C=CC1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-UHFFFAOYSA-N 0.000 claims description 4
- ZZZCUOFIHGPKAK-UHFFFAOYSA-N D-erythro-ascorbic acid Natural products OCC1OC(=O)C(O)=C1O ZZZCUOFIHGPKAK-UHFFFAOYSA-N 0.000 claims description 4
- 229930003268 Vitamin C Natural products 0.000 claims description 4
- FPIPGXGPPPQFEQ-OVSJKPMPSA-N all-trans-retinol Chemical compound OC\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-OVSJKPMPSA-N 0.000 claims description 4
- 210000004027 cell Anatomy 0.000 claims description 4
- 150000002632 lipids Chemical class 0.000 claims description 4
- 235000019154 vitamin C Nutrition 0.000 claims description 4
- 229940045997 vitamin a Drugs 0.000 claims description 4
- 102000015081 Blood Coagulation Factors Human genes 0.000 claims description 3
- 108010039209 Blood Coagulation Factors Proteins 0.000 claims description 3
- 239000003114 blood coagulation factor Substances 0.000 claims description 3
- 150000003839 salts Chemical class 0.000 claims description 3
- 102000004411 Antithrombin III Human genes 0.000 claims description 2
- 108090000935 Antithrombin III Proteins 0.000 claims description 2
- 101710081722 Antitrypsin Proteins 0.000 claims description 2
- 230000001475 anti-trypsic effect Effects 0.000 claims description 2
- 229960005348 antithrombin iii Drugs 0.000 claims description 2
- 210000001772 blood platelet Anatomy 0.000 claims description 2
- 238000002523 gelfiltration Methods 0.000 claims description 2
- 210000003714 granulocyte Anatomy 0.000 claims description 2
- 210000004698 lymphocyte Anatomy 0.000 claims description 2
- 210000002966 serum Anatomy 0.000 claims description 2
- 238000001179 sorption measurement Methods 0.000 claims description 2
- 239000002753 trypsin inhibitor Substances 0.000 claims description 2
- 238000000108 ultra-filtration Methods 0.000 claims description 2
- 238000005406 washing Methods 0.000 claims description 2
- 239000000463 material Substances 0.000 claims 4
- 108060003951 Immunoglobulin Proteins 0.000 claims 1
- 239000007864 aqueous solution Substances 0.000 claims 1
- 239000003914 blood derivative Substances 0.000 claims 1
- 239000003795 chemical substances by application Substances 0.000 claims 1
- 102000018358 immunoglobulin Human genes 0.000 claims 1
- 241000711408 Murine respirovirus Species 0.000 description 20
- 210000002381 plasma Anatomy 0.000 description 19
- 241000700605 Viruses Species 0.000 description 18
- 230000002779 inactivation Effects 0.000 description 18
- 241001529453 unidentified herpesvirus Species 0.000 description 16
- 210000003743 erythrocyte Anatomy 0.000 description 9
- 208000015181 infectious disease Diseases 0.000 description 8
- 230000002458 infectious effect Effects 0.000 description 8
- 239000012620 biological material Substances 0.000 description 5
- 238000002360 preparation method Methods 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- VEZXCJBBBCKRPI-UHFFFAOYSA-N beta-propiolactone Chemical compound O=C1CCO1 VEZXCJBBBCKRPI-UHFFFAOYSA-N 0.000 description 3
- 239000006285 cell suspension Substances 0.000 description 3
- 239000003599 detergent Substances 0.000 description 3
- 238000011534 incubation Methods 0.000 description 3
- 229960000380 propiolactone Drugs 0.000 description 3
- 239000000523 sample Substances 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 229930003270 Vitamin B Natural products 0.000 description 2
- 210000000601 blood cell Anatomy 0.000 description 2
- 238000010790 dilution Methods 0.000 description 2
- 239000012895 dilution Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 235000013601 eggs Nutrition 0.000 description 2
- 230000001717 pathogenic effect Effects 0.000 description 2
- 239000013074 reference sample Substances 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- 235000019156 vitamin B Nutrition 0.000 description 2
- 239000011720 vitamin B Substances 0.000 description 2
- INGWEZCOABYORO-UHFFFAOYSA-N 2-(furan-2-yl)-7-methyl-1h-1,8-naphthyridin-4-one Chemical compound N=1C2=NC(C)=CC=C2C(O)=CC=1C1=CC=CO1 INGWEZCOABYORO-UHFFFAOYSA-N 0.000 description 1
- 206010053567 Coagulopathies Diseases 0.000 description 1
- 102000001690 Factor VIII Human genes 0.000 description 1
- 108010054218 Factor VIII Proteins 0.000 description 1
- 206010018910 Haemolysis Diseases 0.000 description 1
- 102000001554 Hemoglobins Human genes 0.000 description 1
- 108010054147 Hemoglobins Proteins 0.000 description 1
- XQFRJNBWHJMXHO-RRKCRQDMSA-N IDUR Chemical compound C1[C@H](O)[C@@H](CO)O[C@H]1N1C(=O)NC(=O)C(I)=C1 XQFRJNBWHJMXHO-RRKCRQDMSA-N 0.000 description 1
- 102000014150 Interferons Human genes 0.000 description 1
- 108010050904 Interferons Proteins 0.000 description 1
- 102000015696 Interleukins Human genes 0.000 description 1
- 108010063738 Interleukins Proteins 0.000 description 1
- 208000036142 Viral infection Diseases 0.000 description 1
- 150000001242 acetic acid derivatives Chemical class 0.000 description 1
- 230000002924 anti-infective effect Effects 0.000 description 1
- 239000000427 antigen Substances 0.000 description 1
- 102000036639 antigens Human genes 0.000 description 1
- 108091007433 antigens Proteins 0.000 description 1
- 238000003556 assay Methods 0.000 description 1
- 238000004113 cell culture Methods 0.000 description 1
- 230000001413 cellular effect Effects 0.000 description 1
- 239000013043 chemical agent Substances 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 230000035602 clotting Effects 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 239000013068 control sample Substances 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 229960000301 factor viii Drugs 0.000 description 1
- 230000035931 haemagglutination Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 230000008588 hemolysis Effects 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 229940047124 interferons Drugs 0.000 description 1
- 229940047122 interleukins Drugs 0.000 description 1
- 210000000265 leukocyte Anatomy 0.000 description 1
- 238000002941 microtiter virus yield reduction assay Methods 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 230000004962 physiological condition Effects 0.000 description 1
- 229920000136 polysorbate Polymers 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 238000004448 titration Methods 0.000 description 1
- 238000009281 ultraviolet germicidal irradiation Methods 0.000 description 1
- 230000009385 viral infection Effects 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L2/00—Methods or apparatus for disinfecting or sterilising materials or objects other than foodstuffs or contact lenses; Accessories therefor
- A61L2/0005—Methods or apparatus for disinfecting or sterilising materials or objects other than foodstuffs or contact lenses; Accessories therefor for pharmaceuticals, biologicals or living parts
- A61L2/0082—Methods or apparatus for disinfecting or sterilising materials or objects other than foodstuffs or contact lenses; Accessories therefor for pharmaceuticals, biologicals or living parts using chemical substances
- A61L2/0088—Liquid substances
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/045—Hydroxy compounds, e.g. alcohols; Salts thereof, e.g. alcoholates
- A61K31/07—Retinol compounds, e.g. vitamin A
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
- A61K31/35—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom
- A61K31/352—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom condensed with carbocyclic rings, e.g. methantheline
- A61K31/353—3,4-Dihydrobenzopyrans, e.g. chroman, catechin
- A61K31/355—Tocopherols, e.g. vitamin E
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K35/00—Medicinal preparations containing materials or reaction products thereof with undetermined constitution
- A61K35/12—Materials from mammals; Compositions comprising non-specified tissues or cells; Compositions comprising non-embryonic stem cells; Genetically modified cells
- A61K35/14—Blood; Artificial blood
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K35/00—Medicinal preparations containing materials or reaction products thereof with undetermined constitution
- A61K35/12—Materials from mammals; Compositions comprising non-specified tissues or cells; Compositions comprising non-embryonic stem cells; Genetically modified cells
- A61K35/14—Blood; Artificial blood
- A61K35/16—Blood plasma; Blood serum
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L2/00—Methods or apparatus for disinfecting or sterilising materials or objects other than foodstuffs or contact lenses; Accessories therefor
- A61L2/16—Methods or apparatus for disinfecting or sterilising materials or objects other than foodstuffs or contact lenses; Accessories therefor using chemical substances
- A61L2/18—Liquid substances or solutions comprising solids or dissolved gases
Definitions
- the invention relates to a method for sterilization of blood, plasma, blood- and plasma derivatives, cell suspensions or similar with a physiologically innocuous sterilant.
- Human blood or human plasma or derived products potentially entail the risk of transmitting viral infection.
- human pathogenic lipid viruses such as HIV, HNANBV and HBV play a special role. For this reason, preparations derived from human blood or plasma must be virus inactivated.
- Clotting preparations such as F VIII or F IX concentrates can be sterilized by means of heat (EP 0 037 078), but require appreciable amounts of stabilizers in order to stand such a treatment. In other methods, the preparation is heated in the lyophilized state, with additional use of organic solvents, pressure or steam in combination.
- Chemical agents such as a combination of lipid solvents and detergents or beta-propiolactone in combination with UV irradiation (EP 0 014 333) are also used.
- the invention is based on the task of providing a virus inactivation procedure which works under physiological conditions and with physiological substances, which is suitable for sterilization of blood/plasma or their derivatives as well as for cell suspensions.
- a physiologically well-tolerated substance which can remain in the biological material to be sterilized is used as sterilizing agent.
- Vitamins are natural physiological substances of which the anti-infectious, health-promoting activity is already known. Moreover, vitamins do not have to be removed from the biological material to be sterilized, since the human body relies on supply of vitamins.
- Preferred vitamins are vitamin A, B, B 1 , B 6 , B 12 , C and E.
- Preferred salts are the acetates, such as vitamin A- and E-acetate.
- Sterilization is carried out in that the biological material to be sterilized is mixed with 0.01 to 1.0 weight % of a vitamin (per volume% sterilisate) and preferably 0.2%, the pH value is adjusted to 5.6 to 8.5 and incubation is carried out with stirring for up to 24 hours at 10° C. to 50° C.
- the pH value is 7.15 and the temperature is 23° C. to 37° C., and more preferentially 23° C. or 37° C.
- the preferred sterilization time is three to four hours.
- a dissolution mediator can be added to improve the solubility of the vitamin.
- a preferred solubilizer is e.g. Tween 80.
- the method in accordance with the invention enables virus inactivation in blood, blood cells, blood plasma, blood serum, constituents of blood cells (e.g. interferons, interleukins or hemoglobins, red cell concentrates or concentrates of other cellular blood compounds as granulocytes, platelets, lymphocytes etc.) as well as plasma derivatives (e.g. plasma cryopoor plasma, coagulation factors, cryoprecipitate (e.g. factor VIII, IX, X, XIII etc.), immunoglobulines, the inhibitors ⁇ 1 antitrypsin, antithrombin III etc.).
- constituents of blood cells e.g. interferons, interleukins or hemoglobins, red cell concentrates or concentrates of other cellular blood compounds as granulocytes, platelets, lymphocytes etc.
- plasma derivatives e.g. plasma cryopoor plasma, coagulation factors, cryoprecipitate (e.g. factor VIII, IX, X, XIII etc.
- the sterilizing agent i.e. the vitamin
- the sterilizing agent can remain in the biological material to be virus inactivated but it also may easily be removed from the sterilized preparation by means of washing gelfiltration, adsorption or ultrafiltration.
- Sendai viruses were used to demonstrate virus inactivation in accordance with the discovery.
- Sendai viruses have been proved to be very effective in experiments as model viruses for the human pathogenic lipid viruses HBV, HNANBV and HIV.
- Herpes virus HSV-I has been used.
- a reference sample which was also contaminated with Sendai virus was incubated under the same conditions but without addition of the vitamin.
- the samples were frozen immediately after incubation at -80° C.
- the infectious titers of Sendai virus were determined on incubated eggs.
- a titer of 10 2 .7 infectious units/ml was found.
- infectious virus was no longer demonstrated, corresponding to an inactivation of ⁇ 2.7 log 10 .
- Human erythrocytes washed three times with 0.9% sodium chloride, were spiked with Sendai virus (dilution 1:100). 0.25% vitamin E-acetate was added to one aliquot of the virus spiked erythrocytes and the mixture incubated at 37° C. for 3 hours. The second virus spiked aliquot was incubated without vitamin addition. In all the following examples, the control sample was treated identically. Infectious Sendai virus was titrated in embryonated eggs and antigen determined by haemagglutination assay.
- HSV-I Herpes virus
- Herpes virus was titrated on cell culture (Rita-cells) by plaque counting. The results are given in Table II. Tween 80 alone shows almost no virus inactivation activity. Even concentrations ten times higher than those used in the combination with vitamin E are ineffective.
- Human plasma was spiked with Sendai virus (dilution 1:50) and one aliquot of the spiked plasma was incubated in the presence of 0.2% vitamin A acetate at 23° C. for three hours.
- Virus titration was performed as described in Example 1. Treatment with vitamin A acetate resulted in a titer reduction of Sendai virus of >2.7 log 10 (Table III).
- Human plasma was spiked with Sendai virus as described in Example 4 and treated with vitamin A acetate (0.5%) supplemented with Tween 80 (0.15%).
- Human plasma was spiked with Sendai virus and treated with vitamin B 6 (0.2%). Incubation was performed at 23° C. for three hours. Titration of Sendai virus was performed as described above. Titer of infectious Sendai virus was reduced by treatment with vitamin B 6 by >2.7 log 10 (Table IV). Treatment with 0.1% vitamin B 6 resulted in an inactivation of 1.0 log 10 .
- HSV-I Herpes virus
- HSV-I Herpes virus
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Epidemiology (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Cell Biology (AREA)
- Hematology (AREA)
- Biomedical Technology (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Developmental Biology & Embryology (AREA)
- Immunology (AREA)
- Virology (AREA)
- Zoology (AREA)
- Biotechnology (AREA)
- Molecular Biology (AREA)
- General Chemical & Material Sciences (AREA)
- Medicines Containing Material From Animals Or Micro-Organisms (AREA)
- Apparatus For Disinfection Or Sterilisation (AREA)
- External Artificial Organs (AREA)
- Fertilizers (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE3805459 | 1988-02-22 | ||
DE3805459A DE3805459A1 (de) | 1988-02-22 | 1988-02-22 | Verfahren zur sterilisation von blut, plasma, blut- und plasmaderivaten, zellsuspensionen oder dgl. |
Publications (1)
Publication Number | Publication Date |
---|---|
US5011695A true US5011695A (en) | 1991-04-30 |
Family
ID=6347890
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US07/311,483 Expired - Fee Related US5011695A (en) | 1988-02-22 | 1989-02-16 | Sterilization of blood and its derivatives with vitamins |
Country Status (7)
Country | Link |
---|---|
US (1) | US5011695A (enrdf_load_stackoverflow) |
EP (1) | EP0330047B1 (enrdf_load_stackoverflow) |
JP (1) | JPH025957A (enrdf_load_stackoverflow) |
AT (1) | ATE80803T1 (enrdf_load_stackoverflow) |
DE (2) | DE3805459A1 (enrdf_load_stackoverflow) |
ES (1) | ES2035384T3 (enrdf_load_stackoverflow) |
GR (1) | GR3006630T3 (enrdf_load_stackoverflow) |
Cited By (28)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5288605A (en) * | 1992-03-02 | 1994-02-22 | Steritech, Inc. | Methods for inactivating bacteria in blood preparations with 8-methoxypsoralen |
US5418130A (en) * | 1990-04-16 | 1995-05-23 | Cryopharm Corporation | Method of inactivation of viral and bacterial blood contaminants |
US5482828A (en) * | 1992-03-02 | 1996-01-09 | Steritech, Inc. | Synthetic media compositions and methods for inactivating bacteria and viruses in blood preparations with 8-methoxypsoralen |
US5741894A (en) * | 1995-09-22 | 1998-04-21 | Baxter International, Inc. | Preparation of pharmaceutical grade hemoglobins by heat treatment in partially oxygenated form |
US6187572B1 (en) | 1990-04-16 | 2001-02-13 | Baxter International Inc. | Method of inactivation of viral and bacterial blood contaminants |
US6251580B1 (en) | 1992-03-02 | 2001-06-26 | Lily Lin | Synthetic media for blood components |
US6258577B1 (en) | 1998-07-21 | 2001-07-10 | Gambro, Inc. | Method and apparatus for inactivation of biological contaminants using endogenous alloxazine or isoalloxazine photosensitizers |
US6268120B1 (en) | 1999-10-19 | 2001-07-31 | Gambro, Inc. | Isoalloxazine derivatives to neutralize biological contaminants |
US6548241B1 (en) | 2000-11-28 | 2003-04-15 | Gambro, Inc. | Storage solution containing photosensitizer for inactivation of biological contaminants |
US20030215784A1 (en) * | 1998-07-21 | 2003-11-20 | Dumont Larry Joe | Method and apparatus for inactivation of biological contaminants using photosensitizers |
US20040001816A1 (en) * | 1998-06-22 | 2004-01-01 | Cytomedix, Inc. | Enriched platelet wound healant |
US20040018997A1 (en) * | 1998-07-21 | 2004-01-29 | Heather Reddy | Inactivation of West Nile virus and malaria using photosensitizers |
US20040081956A1 (en) * | 2000-06-02 | 2004-04-29 | Gambro, Inc. | Induction of and maintenance of nucleic acid damage in pathogens using riboflavin and light |
EP1091735A4 (en) * | 1998-06-22 | 2004-05-06 | Cytomedix Inc | IMPROVED WOUND HEALING WITH ENRICHED PLATES |
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US20050112021A1 (en) * | 2000-06-15 | 2005-05-26 | Gambro, Inc. | Reduction of Contaminants In Blood and Blood Products Using Photosensitizers and Peak Wavelengths of Light |
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US7094378B1 (en) | 2000-06-15 | 2006-08-22 | Gambro, Inc. | Method and apparatus for inactivation of biological contaminants using photosensitizers |
US20070071740A1 (en) * | 2005-09-27 | 2007-03-29 | Bio-Tissue, Inc. | Purified amniotic membrane compositions and methods of use |
US20070099170A1 (en) * | 1998-07-21 | 2007-05-03 | Navigant Biotechnologies, Inc. | Method for treatment and storage of blood and blood products using endogenous alloxazines and acetate |
US20070098697A1 (en) * | 2000-06-02 | 2007-05-03 | Navigant Biotechnologies, Inc. | Preventing Transfusion Related Complications in a Recipient of a Blood Transfusion |
US7220747B2 (en) | 1999-07-20 | 2007-05-22 | Gambro, Inc. | Method for preventing damage to or rejuvenating a cellular blood component using mitochondrial enhancer |
US20080107636A1 (en) * | 2000-06-02 | 2008-05-08 | Navigant Biotechnologies, Llc | Induction of and Maintenance of Nucleic Acid Damage in Pathogens Using Riboflavin and Light |
US20080299538A1 (en) * | 2003-02-28 | 2008-12-04 | Caridianbct Biotechnologies, Llc | Pathogen Inactivation of Whole Blood |
US20090023130A1 (en) * | 2003-02-28 | 2009-01-22 | Caridianbct Biotechnologies, Llc | Prevention of Transfusion Related Acute Lung Injury Using Riboflavin and Light |
US20130129844A1 (en) * | 2010-07-28 | 2013-05-23 | Horus Pharma | Preservative-Free Composition for Topical Use Including Hyaluronic Acid |
US9044523B2 (en) | 2000-06-15 | 2015-06-02 | Terumo Bct, Inc. | Reduction of contaminants in blood and blood products using photosensitizers and peak wavelengths of light |
EP3875096A4 (en) * | 2018-11-07 | 2022-11-09 | TERUMO Kabushiki Kaisha | METHOD OF PREPARING A BLOOD PRODUCT AND BLOOD PRODUCT |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3930510A1 (de) * | 1989-09-13 | 1991-03-21 | Blutspendedienst Dt Rote Kreuz | Verfahren zur inaktivierung von viren in blut und blutprodukten |
US5242642A (en) * | 1989-11-25 | 1993-09-07 | Seiko Epson Corporation | Method of manufacturing a switch substrate |
JPH03219509A (ja) * | 1989-11-25 | 1991-09-26 | Seiko Epson Corp | スイッチ基板及びスイッチ基板製造方法 |
AR001654A1 (es) * | 1995-04-19 | 1997-11-26 | Univ East Carolina | Método para la descontaminacion microbiana de plaquetas sanguineas |
JP4828126B2 (ja) * | 2005-02-03 | 2011-11-30 | 日本メナード化粧品株式会社 | 抗菌剤 |
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US5482828A (en) * | 1992-03-02 | 1996-01-09 | Steritech, Inc. | Synthetic media compositions and methods for inactivating bacteria and viruses in blood preparations with 8-methoxypsoralen |
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US20070099170A1 (en) * | 1998-07-21 | 2007-05-03 | Navigant Biotechnologies, Inc. | Method for treatment and storage of blood and blood products using endogenous alloxazines and acetate |
US6258577B1 (en) | 1998-07-21 | 2001-07-10 | Gambro, Inc. | Method and apparatus for inactivation of biological contaminants using endogenous alloxazine or isoalloxazine photosensitizers |
US20050282143A1 (en) * | 1998-07-21 | 2005-12-22 | Gambro, Inc. | Use of visible light at wavelengths of 500 nm and higher to pathogen reduce blood and blood components |
US7220747B2 (en) | 1999-07-20 | 2007-05-22 | Gambro, Inc. | Method for preventing damage to or rejuvenating a cellular blood component using mitochondrial enhancer |
US6268120B1 (en) | 1999-10-19 | 2001-07-31 | Gambro, Inc. | Isoalloxazine derivatives to neutralize biological contaminants |
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US20080107636A1 (en) * | 2000-06-02 | 2008-05-08 | Navigant Biotechnologies, Llc | Induction of and Maintenance of Nucleic Acid Damage in Pathogens Using Riboflavin and Light |
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US20070098697A1 (en) * | 2000-06-02 | 2007-05-03 | Navigant Biotechnologies, Inc. | Preventing Transfusion Related Complications in a Recipient of a Blood Transfusion |
US20100080781A1 (en) * | 2000-06-02 | 2010-04-01 | Caridianbct Biotechnologies, Llc | Preventing Transfusion Related Complications in a Recipient of a Blood Transfusion |
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US7094378B1 (en) | 2000-06-15 | 2006-08-22 | Gambro, Inc. | Method and apparatus for inactivation of biological contaminants using photosensitizers |
US20050112021A1 (en) * | 2000-06-15 | 2005-05-26 | Gambro, Inc. | Reduction of Contaminants In Blood and Blood Products Using Photosensitizers and Peak Wavelengths of Light |
US9044523B2 (en) | 2000-06-15 | 2015-06-02 | Terumo Bct, Inc. | Reduction of contaminants in blood and blood products using photosensitizers and peak wavelengths of light |
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US20090023130A1 (en) * | 2003-02-28 | 2009-01-22 | Caridianbct Biotechnologies, Llc | Prevention of Transfusion Related Acute Lung Injury Using Riboflavin and Light |
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Also Published As
Publication number | Publication date |
---|---|
ATE80803T1 (de) | 1992-10-15 |
DE3805459A1 (de) | 1989-08-31 |
DE58902313D1 (de) | 1992-10-29 |
ES2035384T3 (es) | 1993-04-16 |
JPH025957A (ja) | 1990-01-10 |
EP0330047B1 (de) | 1992-09-23 |
GR3006630T3 (enrdf_load_stackoverflow) | 1993-06-30 |
EP0330047A2 (de) | 1989-08-30 |
EP0330047A3 (en) | 1990-12-19 |
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